Oncology Clinical Research Coordinator - Be the Bridge Between Patients and Breakthrough Cancer Therapies If you're energized by fast‑paced clinical work, motivated by helping patients through some of their most vulnerable moments, and excited to support cutting‑edge cancer research, this role places you at the heart of oncology trials that change lives. We're looking for a Clinical Research Coordinator who thrives in a hands‑on environment-someone who can balance compassionate patient care wit…

Covington, LA, United States of America Kenner, LA, United States of America Full time R1566072 This is an on site role and candidate must be able to travel from Covington LA to Kenner LA. Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. Why Avacare? At Avacare, CRCs wear…

Covington, LA, United States of America Kenner, LA, United States of America Full time R1566072 This is an on site role and candidate must be able to travel from Covington LA to Kenner LA. Are you ready to accelerate your career in clinical research? Join Avacare, a dynamic Site Management Organization (SMO) where Clinical Research Coordinators (CRCs) gain unparalleled exposure to diverse trials, hands-on responsibilities, and a collaborative team environment. Why Avacare? At Avacare, CRCs wear…

Job Title: Clinical Research Coordinator Location: West Hills, California Type: Contract Compensation: $26.00-$30.00/hr Work Model: Onsite - onsite Hours: 40.0 Responsibilities Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. Conduct screening visits to collect medical history & other information from study participants. Assist with informed consent and enrollment of study participants in accordance with protoc…

Job Title: Clinical Research Coordinator Location: Las Vegas, NV Type: Contract Compensation: $30.00/hr Work Model: Onsite Hours: 40 hours Responsibilities Assist in the coordination and execution of clinical research protocols under the supervision of the PI and senior research staff. Conduct screening visits to collect medical history & other information from study participants. Assist with informed consent and enrollment of study participants in accordance with protocol requirements and e…

Job Title: Oncology Clinical Research Coordinator This is a fully onsite position in Chapel Hill,NC; relocation required Job Description This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. Responsibilities Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closu…

Job Title: Oncology Clinical Research Coordinator This is a fully onsite position in Chapel Hill,NC; relocation required Job Description This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. Responsibilities Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closu…

Job Title: Oncology Clinical Research Coordinator This is a fully onsite position in Chapel Hill,NC; relocation required Job Description This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. Responsibilities Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closu…

Job Title: Clinical Research Coordinator Job Description This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. Responsibilities Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closure. Recruit, screen, consent, and enroll study participants. Schedule and mana…

Job Title: Oncology Clinical Research Coordinator This is a fully onsite position in Chapel Hill,NC; relocation required Job Description This position involves independently managing multiple oncology clinical trials from startup through closeout while serving as the primary point of contact between patients, physicians, sponsors, research staff, and clinical teams. Responsibilities Coordinate all phases of clinical trials, including activation, enrollment, conduct, monitoring, and study closu…

Our team members are the heart of what makes us better. At Hackensack Meridian _Health_ we help our patients live better, healthier lives - and we help one another to succeed. With a culture rooted in connection and collaboration, our employees are team members. Here, competitive benefits are just the beginning. It's also about how we support one another and how we show up for our community. Together, we keep getting better - advancing our mission to transform healthcare and serve as a leader o…

Job Title: Clinical Research CoordinatorJob Description We are seeking a dedicated Clinical Research Coordinator to manage the initiation and activation of new clinical trial protocols. This role involves coordinating various aspects of the study process, ensuring compliance with all regulatory requirements, and maintaining meticulous research records. Responsibilities Verify Scientific Review Board (SRB), Institutional Review Board (IRB), Human Research Oversight Committee (HROC), data collec…

Job Title: Associate Clinical Research Coordinator (Contractor) Job Description The Associate Clinical Research Coordinator contractor supports clinical research operations by coordinating non-therapeutic clinical research protocols, assisting with participant-facing activities, and ensuring accurate study documentation in a highly regulated environment. Working under the direction of a principal investigator, supervisor, and other research staff, this role helps facilitate efficient, compliant…

Job Title: Clinical Clinical Research Coordinator (Contractor) Job Description The Associate Clinical Research Coordinator contractor supports clinical research operations by coordinating non-therapeutic clinical research protocols, assisting with participant-facing activities, and ensuring accurate study documentation in a highly regulated environment. Working under the direction of a principal investigator, supervisor, and other research staff, this role helps facilitate efficient, compliant,…

Job Title: Clinical Research Coordinator HematologyJob Description The Clinical Research Coordinator Hematology supports complex drug clinical trials by working directly with patients in a hematology-focused research setting. This role coordinates patient visits, conducts patient-facing research activities, and collaborates closely with research nurses and specialized disease-based teams. The coordinator contributes to patient recruitment, screening, and consent, and ensures accurate documentat…

Position Objective: Provide services as a Clinical Research Coordinator in support of the overall functions of the National Institute of Neurological Disorders and Stroke (NINDS) within the National Institutes of Health (NIH). Coordinate the functions necessary for recruitment, scheduling, travel, outpatient admission, and inpatient admission of patients to the Clinical Center, to include acting as a liaison between the patient/family and the ME/CFS/GWI research team, and interaction with the m…

Saint Luke's Hospital | 4401 Wornall Rd | Kansas City | MO Full time JobReq0060441 Job Description Saint Luke's Hospital in Kansas City, MO is seeking a Research Coordinator to join our research team to assist with providing and coordinating care for patients active in various research studies. As a Clinical Research Coordinator in this position, you will prepare the site for conduct of the study identify potential study participants, conduct informed consent, assist with scheduling labs and ap…

Work Schedule Standard Office Hours (40/wk) Environmental Conditions Able to lift 40 lbs. without assistance, Cold Room/Freezers -22degreesF/-6degrees C, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Join us as Clinical Research Coordinator - And manage the day-to-day operations of our clinical trials. What You'll Do: - Conduct multiple ongoing clinical trials, of varying size and complexity, invol…

Work Schedule Standard (Mon-Fri) Environmental Conditions Able to lift 40 lbs. without assistance, Laboratory Setting, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.) Job Description Join us as a Clinical Research Coordinator II - And play a key role in overseeing clinical site activities and ensuring high standards of patient care and data integrity. What You'll Do: - Conduct clinical studies according to FDA/GCP a…

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description Join us as a Clinical Research Coordinator I - To coordinate and manage clinical trials, ensuring adherence to protocols, regulatory requirements, and timelines while working closely with the clinical team to support patient recruitment, data collection, and documentation efforts for advancing medical research. At Thermo Fisher Scientific, you'll discover meaningful work that makes a positive impact on a global sca…